弯蕊开口箭中的多羟基甾体皂甙元

从弯蕊开口箭(Tupistra wattii Hook．f．)的新鲜根茎中分离出2个新的多羟基甾体皂甙元,分别命名为弯蕊皂甙元B(wattigenin B)(1)和弯蕊皂甙元C(wattigenin C)(2),同时分离到2个已知的甾体皂甙元——凯替皂甙元kitigenin(3)和铃兰皂甙元B(convallagenin B)(4)。通过波谱解析鉴定了这4个皂甙元的结构,并测定了它们在体外对肿瘤细胞K562和A2780a的细胞毒活性。化合物1～4为首次从该种植物中分离得到。     

弯蕊开口箭中一个新的甾体皂甙元

从云南民间抗炎药弯蕊开口箭（Ｔｕｐｉｓｔｒａ ｗａｔｔｉｉ Ｈｏｏｋ．ｆ．）的新鲜根状茎中分离到１个新的甾体皂甙元,命名为弯蕊开口箭甙元Ａ（ｗａｔｔｉｇｅｎｉｎ Ａ）,其结构通过光谱分析鉴定为螺甾－２５（２７）－烯－１β,２β,３β,４β,５β,６β－六醇;同时还分离到１个已知的甾体皂甙元,兰茂甙元Ｄ（ｒａｎｍｏｇｅｎｉｎＤ）。     

弯蕊开口箭中的多羟基甾体皂甙元

从弯蕊开口箭(Tupistra wattii Hook. f.)的新鲜根茎中分离出2个新的多羟基甾体皂甙元,分别命名为弯蕊皂甙元B (wattigenin B) (1) 和弯蕊皂甙元C (wattigenin C) (2), 同时分离到2个已知的甾体皂甙元--凯替皂甙元kitigenin (3)和铃兰皂甙元B (convallagenin B) (4).通过波谱解析鉴定了这4个皂甙元的结构,并测定了它们在体外对肿瘤细胞K562和A2780a的细胞毒活性.化合物1～4为首次从该种植物中分离得到.     

晚香玉球茎中的一个新胆甾烷类配糖体

从晚香玉(Polianthes tuberosa L.)球茎中分离到3个胆甾烷类配糖体。经波谱分析鉴定,其中1个为新的胆甾烷类配糖体,即(22S)—胆甾烷-5-烯-1β,3β,16β,22,25-五醇1—O—β-D-葡萄毗喃糖基—16—O-β-D芹菜呋喃糖苷。     

开口箭根茎中甾体化合物的研究

从开口箭根茎部位共分离得到9个甾体化合物,经波谱数据分析结合文献对照分别鉴定为3-epi-neoruscogenin-3-β-D-glucopyranoside(1),3-epi-ruscogenin-3-β-D-glucopyranoside(2),ranmogenin A(3),convallagenin B(4),3-epi-neoruscogenin(5),tupichigenin E(6),(20S,22R)-spirost-25(27)-ene-1β,2β,3β,4β,5β,7α-hexaol-6-one(7),β-谷甾醇(8)和胡萝卜苷(9)。其中化合物1、2和4为首次从该植物中分离得到。     

五种开口箭属植物根状茎中甾体皂甙元的初步研究

薄层层析结果显示五种开口箭属植物根状茎中均含有甾体皂甙和甾体皂甙元,为开口箭属植物作为甾体药物资源提供了依据。     

五种开口箭属植物根状茎中甾体皂甙及甾体皂甙元的初步研究

薄层层析结果显示五种开口箭属植物根状茎中均含有甾体皂甙和甾体皂甙元 ,为开口箭属植物作为甾体药物资源提供了依据。     

徐长卿中的一个新的C21甾体配糖体

从传统中药徐长卿（Cynanchum paniculatum Ktag)根茎的乙酸乙酯提取物中分离得到1个新的C21甾体配糖体,经1D,2D-NMR波谱分析,确定其结构为新白薇甙元C3-O-β-D-夹竹桃吡喃糖甙（1）。     

开口箭甾体皂甙元的分离鉴定及其抗荔枝霜疫霉菌活性

在以荔枝霜疫霉菌为指示菌的生物活性测定导向跟踪下,运用TLC、硅胶柱层析、反相硅胶柱层析和凝胶柱层析等分离纯化方法,从开口箭(Tupistra chinensis)甲醇提取物的乙酸乙酯分部萃取物中分离纯化得到2个抗菌化合物。经现代光谱(MS、IR、1D NMR和2D NMR)分析,确定化合物1为1β,2β,3β,4β,5β,7α-六羟基螺甾-25(27)-烯-6-酮,化合物2为螺甾-25(27)-烯-1β,2β,3β,4β,5β,6β,7α-七醇。离体抗菌活性测定化合物1和化合物2抑制荔枝霜疫霉菌(Peronophythora litchii)孢子囊萌发的EC50分别为100.28 mg.mL-1和124.37 mg.mL-1。用质量浓度为500 mg.mL-1的两个化合物分别处理后接种霜疫霉菌,供试荔枝果实的发病率分别为16.7%和18.9%。     

长缘厚朴中的新配糖体

从长缘厚朴（Magnolia rostrata W.W.Smith)干燥树皮的乙醇提取物中分离得到一个新的配糖体,1,1'－联苯－6',8',9'-三羟基－3－丙基－4－O－β－D吡喃葡萄糖苷（1）,以及6个已知的苯丙素类配糖体,3,4－二羟基－烯丙基－3－O－α－L－吡喃鼠李糖（1→6）β－D－吡喃葡萄糖苷（2）,3,4－二羟基－烯丙基苯－3－O－α－L－吡鼠李糖（1→2）β－D－吡喃葡萄糖苷（3）,sinapaldehyde(E)-O-β-D-glucopyranoside(4),syringaresinol-di-O-β-D-glucopynanoside(5),A阿克苷（E）（6）,IcarisideE5(7),经光谱和化学方法鉴定其结构。     

川麦冬中的新C_(27)甾体甙(英文)

从百合科植物川麦冬 (OphiopogonjaponicusKer_Gawl.)块根中分离得到 4个C2 7甾体甙类化合物 ,其中两个为新化合物 :ophiopojaponinA ( 1)和B ( 2 )。它们的结构通过波谱和化学方法鉴定为 :pennogenin 3_O_[2′_O_acetyl_α_L_rhamnopyranosyl ( 1→ 2 ) ]_β_D_xylopyranosyl ( 1→ 3)_β_D_glucopyranoside ( 1) ,2 6_O_β_D_glucopyranosyl_( 2 2 ξ,2 5R)_3β ,14α ,2 2 ξ ,2 6_tetrahydroxyfurost_5_ene 3_O_α_L_rhamnopyranosyl ( 1→ 2 )_β_D_glucopyranoside ( 2 ) ,diosgenin 3_O_[α_L_rhamnopyra nosyl( 1→ 2 ) ]_β_D_xylopyrano_syl ( 1→ 3)_β_D_glucopyranoside ( 3)andruscogenin 1_O_[α_L_rhamnopyranosyl( 1→ 2 ) ]_β_D_xy lopyranosyl ( 1→ 3)_β_D_fucopyranoside ( 4)。     

New Steroidal Glycosides from Ophiopogon japonicus

Two new C 27 steroidal glycosides, named ophiopojaponin A (1) and B (2), together with two known ones, were isolated from the tubers of the famous traditional Chinese herb Ophiopogon japonicus Ker-Gawl. The spectroscopic and chemical evidence revealed their structures to be pennogenin 3-O-［2′-O-acetyl-α-L-rhamnopyranosyl (1→2)］-β-D-xylopyranosyl (1→3)-β-D-glucopyranoside (1), 26-O-β-D-glucopyranosyl-(22ξ, 25R)-3β,14α,22ξ, 26-tetrahydroxyfurost-5-ene 3-O-α-L-rhamnopyranosyl (1→2)-β-D-glucopyranoside(2), diosgenin 3-O-［α-L-rhamnopyranosyl (1→2)］-β-D-xylopyrano-syl (1→3)-β-D-glucopyranoside (3) and ruscogenin 1-O-［α-L-rhamnopyranosyl (1→2)］-β-D-xylopyranosyl (1→3)-β-D-fucopyranoside (4).     

通光藤甙F,G,H和I结构

从通光藤(Marsdeniatenacissima)的茎中分离得到4个新的C21甾体甙———通光藤甙F(3),G(4),H(5)和I(6),以及2个已知化合物通光藤甙A(1)和B(2)。根据光谱数据和化学方法推定了其结构。同时,通过COLOC谱和二维核磁共振谱指定了这些化合物中甙元上11和12位的酯基确切连接位置。     

Steroidal glycosides from Ruscus ponticus

A comparative metabolite profiling of the underground parts and leaves of Ruscus ponticus was obtained by an HPLC-ESIMSⁿ method, based on high-performance liquid chromatography coupled to electrospray positive ionization multistage ion trap mass spectrometry. The careful study of HPLC-ESIMSⁿ fragmentation pattern of each chromatographic peak, in particular the identification of diagnostic product ions, allowed us to get a rapid screening of saponins belonging to different classes, such as dehydrated/or not furostanol, spirostanol and pregnane glycosides, and to promptly highlight similarities and differences between the two plant parts. This approach, followed by isolation and structure elucidation by 1D- and 2D-NMR experiments, led to the identification of eleven saponins from the underground parts, of which two dehydrated furostanol glycosides and one new vespertilin derivative, and nine saponins from R. ponticus leaves, never reported previously. The achieved results highlighted a clean prevalence of furostanol glycoside derivatives in R. ponticus leaves rather in the underground parts of the plant, which showed a wider structure variety. In particular, the occurrence of dehydrated furostanol derivatives, for the first time isolated from a Ruscus species, is an unusual finding which makes unique the saponins profile of R. ponticus.     

Polyhydroxylated steroidal constituents from the fresh rhizomes of Tupistra yunnanensis

Six new polyhydroxylated steroidal saponins, tupistrosides A-F (1-6), together with nine known steroids, were isolated from the fresh rhizomes of Tupistra yunnanensis. Their structures were elucidated to be (25S)-1beta,4beta,5beta-trihydroxy-spirostane-3beta-yl O-alpha-l-arabinopyranoside (1), 1beta,24beta-dihydroxy-spirost-5,25(27)-dien-3alpha-yl O-beta-d-glucopyranoside (2), (22S,25S)-1alpha,2beta,3alpha,5alpha-tetrahydroxy-furo-spirostane-26-yl O-beta-d-glucopyranoside (3), 1beta,3alpha,22 xi-trihydroxy-furost-5,25(27)-dien-26-yl O-beta-d-glucopyranoside (4), 26-O-beta-d-glucopyranosyl-1beta,22-dihydroxy-furost-5-en-3alpha-yl O-beta-d-glucopyranoside (5) and 22-methoxy-1beta,2beta,3beta,4beta,5beta,7alpha-hexahydroxy-furost-25(27)-en-6-one-26-yl O-beta-d-glucopyranoside (6), respectively, by means of spectroscopic analysis and the results of acid hydrolysis.